# FDA Inspection 1003949 - Bricon Technology GmbH - February 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/bricon-technology-gmbh/21f5ce53-e2fd-4cbc-a676-86b2c06344e6
Source feed: FDA_Inspections

> FDA Inspection 1003949 for Bricon Technology GmbH on February 02, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003949
- Company Name: Bricon Technology GmbH
- Inspection Date: 2017-02-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/bricon-technology-gmbh/1f77cf14-5aeb-4768-9c2f-475f4a99c961

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7